A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514250



Internal ID20887602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65548510..65561322hg38UCSC Ensembl
chr15:65840848..65853660hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3812813
hg1912813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025374
Samples
Known GenesPTPLAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514250
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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